Patricia Dewey 480-***-****
**** * ***** *****, **********, AZ 85250 **************@*****.***
PROFILE AND QUALIFICATIONS
Customer service focused support specialist with 14 years career experience supporting clinical trial data collection software. Highly skilled in the following areas: technical support, device configuration & shipping and product testing. Each of these have environments have helped to develop:
Superior organizational skills
Ability to work cohesively within a team
Consistently positive attitude
Respectful and responsible nature
Proficiency in MS Office suite
Familiar with Atalassian’s Jira ticket management system.
Ability to recognize where new processes are needed for improving efficiency then developing or assisting in developing these processes
Strong attention to detail
Fluent in English and French
Professional Experience
assisTek (Formerly Assist Technologies), Scottsdale, AZ
assisTek is an electronic data capture company for medical clinical drug trials. Data was captured on Nexus 7 devices (site based and field based) running the Android OS.
01 May 2002 – present
QA Testing Technician
Responsibilities:
Wrote and updated test cases following technical specifications.
Executed test plans, logged any deviations from expected results into the appropriate Jira tickets.
Wrote traceability matrix.
Data Analyst
Responsibilities:
On a daily basis, verified subject data according to protocol that data was recorded correctly running reports from web-based customer data portal.
Compared data from database with final study results.
Completed data changes for Data Charge Request for Approval (DCRA) and verified that data matched SQL database.
Senior Product Support Specialist
Responsibilities:
Manage Product Support Department
Mentor and train internal staff
Manage Data Change process
Create checklists to ensure processes are carried out in accordance with SOPs
24/7 bi-lingual technical support (English/French)
Assist Clinical Research Organization (CROs) and Site Coordinators with product related questions
Provided remote training for clinical site staff (globally)
Validated translation of psychometric questionnaires
Quality control and document administrator in an FDA regulated (21 CRF part 11) environment
Computer configuration and troubleshooting.
Verify data to ensure accuracy and compliance with protocol
Made sure the company was ready for internal audits with the sponsor of a clinical study.
Document and follow up on any issue received during a product support call/email using Help Desk Authority (HDA) system.
Create internal users on web-based customer portal as well as well as external sponsor users.
Inventory Management
Responsibilities:
Managed Shipping/receiving/tracking for company devices (total of 2500 devices)
International shipment specialist.
Translation coordinator
Disaster Recovery